How can we solve for a X-linked trait gene problem? . If a heterozygous parent (AB/ab) is testcrossed to a homozygous recessive (ab/ab), what will the progeny phenotypic ratio be if genes A and B are completely linked

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A certain type of deafness in humans is inherited as an X-linked recessive trait. A man with this type of deafness married a normal woman, and they are expecting a child. They find out that they are distantly related. Part of the family tree is shown here.How would you advise the parents about the probability of their child being a deaf boy, a deaf girl, a normal boy, or a normal girl? Be sure to state any assumptions that you make.

One family is shown in both pedigrees below. Each pedigree focuses on a different monogenic, fully penetrant phenotype. Shaded individuals affected by Phenotype 1: 3 Shaded individuals affected by Phenotype 2: a. Phenotype 1: Which modes of inheritance can be ruled out, base don't this pedigree? For each mode of inheritance listed below, either state that it is not ruled out, or describe a detail of the pedigree that allows you to rule it out. Autosomal recessive Autosomal dominant X-linked recessive X-linked dominant Y-linked b. Phenotype 2: Which modes of inheritance can be ruled out, base don't this pedigree? For each mode of inheritance listed below, either state that it is not ruled out, or describe a detail of the pedigree that allows you to rule it out. Autosomal recessive Autosomal dominant X-linked recessive X-linked dominant

Tomato Plants In tomato plants, round fruit (R) is dominant to oval fruit (r). Pure breeding plants with red and round fruit (FFRR) were crossed to pure breeding plants with yellow and oval fruit (ffrr). The red and round F1 progeny were then testcrossed to plants that were homozygous recessive for both genes (ffrr) with the following results: Phenotypes Number of Offspring Red and round 2 255 Red and oval 290 Yellow and round 310 Yellow and oval 2 145 Part A: Record the phenotypes and the phenotype ratio in lowest terms. Part B: Convert the expected phenotypic ratio from Part A into the expected probability for each of the four phenotypes and record them in the table below. Calculate the probability for each of the four phenotypes observed in the cross from the data presented at the beginning of the question by dividing the number of progeny in each class by the total number of progeny and record these in the table below. (Probability = Number of Progeny in Phenotype…

What is the approximate percentage chance that individual V.2, shown in the pedigree diagram below will have inherited the X- linked recessive allele shown to be carried by his great-great-grandmother? Note: only type the number, not the percentage symbol. Answer: The chance that individual V.2 shown in the pedigree below has inherited the X-linked recessive allele shown to be carried by his great-great grandmother is approximately Blank 1 percent. 노 ㅍ먹이 12 I 마일 메인 de 먹어 요 58 ㅁ + ܡܐ

Tomato Plants In tomato plants, round fruit (R) is dominant to oval fruit (r). Pure breeding plants with red and round fruit (FFRR) were crossed to pure breeding plants with yellow and oval fruit (ffrr). The red and round F1 progeny were then testcrossed to plants that were homozygous recessive for both genes (ffrr) with the following results: Phenotypes Number of Offspring Red and round 2 255 Red and oval 290 Yellow and round 310 Yellow and oval 2 145 Complete a Punnett square to determine the expected testcross progeny on the basis of Mendel’s Law of Independent Assortment. Record the phenotypes and the phenotype ratio in lowest terms.

Suppose you are testing the null hypothesis that the mode of inheritance for a particular disease in elegant cranes is sex-linked recessive. You employ the following crosses, where R is the wild-type allele, r is the disease allele, and Y is Y-chromosome allele (only in males): Parental cross (Affected male with unaffected (carrier) female): rY x Rr. F₁ cross (Unaffected male with affected female): RY x rr. Suppose you perform these crosses at two different research locations. You obtain the following counts in the F2 generation: Location 01 Male, Disease: 200 Male, Wild-type: 225 Female, Disease: 211 Female, Wild-type: 205, Location 02 Male, Disease: 320 Male, Wild-type: 325 Female, Disease: 354 Female, Wild-type: 310 Do you reject or not reject the null hypothesis that the mode of inheritance is sex-linked recessive at each location? The significance level is 0.01. (Hint: when applying the ChiSq goodness of fit test, if the expected value for a row is 0, remove that row and reduce…